Venous and Lymphatic Disorders Flashcards
(60 cards)
Peripheral vascular disease denotes disorders of peripheral vessels including ………………………………(5).
Peripheral vascular disease denotes disorders of peripheral vessels including arteries, arterioles, veins, venules, and lymphatics.
Vascular lesions may result from ………. vascular pathology or occur ………………… to conditions originating in …………… tissues or organ systems.
Resultant conditions may remain asymptomatic with little or no effect on morbidity and mortality or progress to become life threatening.
Vascular lesions may result from primary vascular pathology or occur secondary to conditions originating in unrelated tissues or organ systems. Resultant conditions may remain asymptomatic with little or no effect on morbidity and mortality or progress to become life threatening.
TECHNIQUES USED TO EVALUATE VENOUS AND LYMPHATIC DISEASE
Angiography
Angiography is the gold standard for evaluating peripheral vascular diseases due to its ability to characterize and visualize normal and abnormal vascular anatomy.[1] Diagnostic outcome requires careful attention to three important elements: selection of radiopaque contrast agent, technique for vascular delivery of contrast material, and high-quality radiographic imaging.
Factors to be considered when selecting a contrast agent include patient safety, image quality, and cost. Reports of adverse side effects to intravenous contrast agents are limited to two dogs that developed acute and severe systemic reactions to iothalamate meglumine.[2] The features of safety and efficacy are somewhat related to the ionic composition of these materials. High-osmolar ionic compounds include the diatrizoate and iothalamate salts (Conray, Renografin). Low-osmolar nonionic compounds include iohexol (Omnipaque), iopamidol (IsoVue), ioversol (Optiray), iopromide (Ultravist), iobitridol (Xenetix), and iomeprol (Iomeron). Low-osmolar ionic compounds include ioxaglate (Hexabrix). Lower-osmolar agents, both ionic and nonionic, are generally tolerated best by patients, particularly those sensitive to an increase in intravascular volume or having advanced cardiac disease (high-osmolar compounds can generate a greater osmotic load).[3] Nonionic agents also have reduced risk of contrast-related anaphylactoid reactions such as urticaria, flushing, coughing, dyspnea, peripheral edema, and a sudden drop in blood pressure.[4],[5] Contrast-related nephrotoxicity is independent of the contrast agent used but can be reduced by maintaining appropriate patient hydration and minimizing the dose of contrast agent used during the imaging study.[6] Low-osmolar agents are generally considerably more expensive than high-osmolar agents.
Venous angiography is generally less challenging than arterial angiography owing to easier access and lower pressures of the venous system. A small intravenous line is placed in a superficial vein distal to the site of the vascular lesion and contrast material is injected. Images are acquired using mechanical rapid film changers or digitally. The advantages of digital angiography include rapid rate of acquisition, postprocessing capabilities, and reduced exposure to radiation.[1] Digital subtraction angiography may be employed to cancel out portions of an image and thereby improve visualization of structures of interest. Computed tomography (CT) angiography is a fast and invasive procedure that fills simultaneous venous structures with a single peripheral venous injection and has replaced conventional venous angiography in people in most applications. Helical CT and three-dimensional CT angiography have been used in dogs to identify portosystemic vasculature and the identification of vascular shunts.
TECHNIQUES USED TO EVALUATE VENOUS AND LYMPHATIC DISEASE
Angiography
Angiography is the gold standard for evaluating peripheral vascular diseases due to its ability to characterize and visualize normal and abnormal vascular anatomy.[1] Diagnostic outcome requires careful attention to three important elements: selection of radiopaque contrast agent, technique for vascular delivery of contrast material, and high-quality radiographic imaging.
Factors to be considered when selecting a contrast agent include patient safety, image quality, and cost. Reports of adverse side effects to intravenous contrast agents are limited to two dogs that developed acute and severe systemic reactions to iothalamate meglumine.[2] The features of safety and efficacy are somewhat related to the ionic composition of these materials. High-osmolar ionic compounds include the diatrizoate and iothalamate salts (Conray, Renografin). Low-osmolar nonionic compounds include iohexol (Omnipaque), iopamidol (IsoVue), ioversol (Optiray), iopromide (Ultravist), iobitridol (Xenetix), and iomeprol (Iomeron). Low-osmolar ionic compounds include ioxaglate (Hexabrix). Lower-osmolar agents, both ionic and nonionic, are generally tolerated best by patients, particularly those sensitive to an increase in intravascular volume or having advanced cardiac disease (high-osmolar compounds can generate a greater osmotic load).[3] Nonionic agents also have reduced risk of contrast-related anaphylactoid reactions such as urticaria, flushing, coughing, dyspnea, peripheral edema, and a sudden drop in blood pressure.[4],[5] Contrast-related nephrotoxicity is independent of the contrast agent used but can be reduced by maintaining appropriate patient hydration and minimizing the dose of contrast agent used during the imaging study.[6] Low-osmolar agents are generally considerably more expensive than high-osmolar agents.
Venous angiography is generally less challenging than arterial angiography owing to easier access and lower pressures of the venous system. A small intravenous line is placed in a superficial vein distal to the site of the vascular lesion and contrast material is injected. Images are acquired using mechanical rapid film changers or digitally. The advantages of digital angiography include rapid rate of acquisition, postprocessing capabilities, and reduced exposure to radiation.[1] Digital subtraction angiography may be employed to cancel out portions of an image and thereby improve visualization of structures of interest. Computed tomography (CT) angiography is a fast and invasive procedure that fills simultaneous venous structures with a single peripheral venous injection and has replaced conventional venous angiography in people in most applications. Helical CT and three-dimensional CT angiography have been used in dogs to identify portosystemic vasculature and the identification of vascular shunts.
These techniques are often selected to detect venous clots (appearing as vascular filling defects) or stenosis. The presence of prolific collateral vasculature can indicate chronic obstruction. Contrast venography of the cranial and caudal vena cava can be performed to assess caval patency, which may be affected by a variety of neoplastic, compressive, or thrombotic disorders.
Lymphangiography helps to permit local assessment of the lymphatic system. The technique of indirect lymphangiography relies on a contrast agent infused into tissue, to be selectively absorbed and transported through lymphatic channels.[9] Direct lymphography is more challenging (unless lymphangiectases have formed) but provides superior results when successfully performed. Selective lymphatic cannulation requires aseptic cutdown over the lymphatic region of interest (note—the identification of lymphangiectases may be facilitated by subcutaneous injection of vital dyes [e.g., 3% Evans blue dye or 11% patent blue violet] into the toe web. By selective resorption of these dyes, the main lymphatic channels proximal to the metacarpus or metatarsus become grossly outlined). The lymphatic vessel is then cannulated with a 27- or 30-gauge needle or a special lymphatic cannula.[9] An iodine-containing soluble contrast medium such as sodium and meglumine diatrizoate (Renografin, Hypaque) is injected slowly into the vessel. Because water-soluble contrast media rapidly diffuse through lymphatic walls into surrounding tissues, the radiographic detail is blurred unless radiographs are taken shortly after dye injection. Alternatively, oily iodine-containing contrast agents (Lipiodol) are used, reducing leakage of contrast from the lymphatic vessels. The oily contrast agents are sequestered within the lymphatics and lymph nodes along the draining pathways.[1] Patency of the lymphatic channels can be appreciated in addition to the size of regional lymph nodes. Metastatic disease to the lymph nodes or granulomas appears as filling defects within the contrast-filled node. Lymphangiography can also be used to identify the location of lymphatic leakage and thoracic duct location in small animals with chylous effusion.[10]
These techniques are often selected to detect venous clots (appearing as vascular filling defects) or stenosis. The presence of prolific collateral vasculature can indicate chronic obstruction. Contrast venography of the cranial and caudal vena cava can be performed to assess caval patency, which may be affected by a variety of neoplastic, compressive, or thrombotic disorders.
Lymphangiography helps to permit local assessment of the lymphatic system. The technique of indirect lymphangiography relies on a contrast agent infused into tissue, to be selectively absorbed and transported through lymphatic channels.[9] Direct lymphography is more challenging (unless lymphangiectases have formed) but provides superior results when successfully performed. Selective lymphatic cannulation requires aseptic cutdown over the lymphatic region of interest (note—the identification of lymphangiectases may be facilitated by subcutaneous injection of vital dyes [e.g., 3% Evans blue dye or 11% patent blue violet] into the toe web. By selective resorption of these dyes, the main lymphatic channels proximal to the metacarpus or metatarsus become grossly outlined). The lymphatic vessel is then cannulated with a 27- or 30-gauge needle or a special lymphatic cannula.[9] An iodine-containing soluble contrast medium such as sodium and meglumine diatrizoate (Renografin, Hypaque) is injected slowly into the vessel. Because water-soluble contrast media rapidly diffuse through lymphatic walls into surrounding tissues, the radiographic detail is blurred unless radiographs are taken shortly after dye injection. Alternatively, oily iodine-containing contrast agents (Lipiodol) are used, reducing leakage of contrast from the lymphatic vessels. The oily contrast agents are sequestered within the lymphatics and lymph nodes along the draining pathways.[1] Patency of the lymphatic channels can be appreciated in addition to the size of regional lymph nodes. Metastatic disease to the lymph nodes or granulomas appears as filling defects within the contrast-filled node. Lymphangiography can also be used to identify the location of lymphatic leakage and thoracic duct location in small animals with chylous effusion.[10]
CT lymphangiography has been used in people to evaluate the lymphatic structures and has been also used in dogs to evaluate the thoracic duct anatomy prior to surgery. Improved identification of lymphatic branches and digital subtraction of superimposing anatomic structures are two benefits seen with CT lymphangiography over radiographic lymphangiography.[10]
CT lymphangiography has been used in people to evaluate the lymphatic structures and has been also used in dogs to evaluate the thoracic duct anatomy prior to surgery. Improved identification of lymphatic branches and digital subtraction of superimposing anatomic structures are two benefits seen with CT lymphangiography over radiographic lymphangiography.[10]
Diagnostic Ultrasound
Ultrasound imaging provides a direct, noninvasive technique for assessing anatomic abnormalities, vascular patency, and function.[11],[12] Ultrasound can aid in the diagnosis of venous thrombosis, aneurysms, traumatic vascular disease, and compression of vascular structures from local disease processes.
Duplex ultrasonography incorporates gray-scale two-dimensional imaging, with pulsed and color flow Doppler techniques. Thrombi, foreign bodies, compression, and abnormal vascular anatomy can be identified with two-dimensional imaging. Color Doppler superimposed on the two-dimensional image can further help define anatomy and identify turbulence associated with vascular malformation and stenotic lesions.[13]
Diagnostic Ultrasound
Ultrasound imaging provides a direct, noninvasive technique for assessing anatomic abnormalities, vascular patency, and function.[11],[12] Ultrasound can aid in the diagnosis of venous thrombosis, aneurysms, traumatic vascular disease, and compression of vascular structures from local disease processes.
Duplex ultrasonography incorporates gray-scale two-dimensional imaging, with pulsed and color flow Doppler techniques. Thrombi, foreign bodies, compression, and abnormal vascular anatomy can be identified with two-dimensional imaging. Color Doppler superimposed on the two-dimensional image can further help define anatomy and identify turbulence associated with vascular malformation and stenotic lesions.[13]
DISEASES OF VEINS
Diseases of the venous system frequently cause …….. clinical problems, despite the fact that veins are commonly affected by or involved in trauma, thromboembolism, edema, local inflammation, and septic processes. Many conditions, however, often go unrecognized. Venous disorders include………..?
DISEASES OF VEINS
Diseases of the venous system frequently cause minor clinical problems, despite the fact that veins are commonly affected by or involved in trauma, thromboembolism, edema, local inflammation, and septic processes. Many conditions, however, often go unrecognized.
Venous disorders include traumatic injuries, superficial and deep phlebitis and thrombosis (thrombophlebitis), catheter embolization, aneurysms, venous compression syndromes, and varicose.
Venous thrombi formed in the venous circulation under low blood flow conditions are composed of …….. and ………….. (Figure 256-1) and have been termed “……… thrombi.”
Venous thrombi formed in the venous circulation under low blood flow conditions are composed of fibrin and erythrocytes (Figure 256-1) and have been termed “red thrombi.”
Venous thrombosis frequently causes fewer clinical abnormalities than arterial thrombosis and, consequently, is often undetected.
Deep venous thrombosis, a major risk factor for …………………. thromboembolism in over 90% of cases in humans, is ………… to be a risk factor for pulmonary thromboembolism in animals.
Venous thrombosis frequently causes fewer clinical abnormalities than arterial thrombosis and, consequently, is often undetected.
Deep venous thrombosis, a major risk factor for pulmonary thromboembolism in over 90% of cases in humans, is not known to be a risk factor for pulmonary thromboembolism in animals.
Pulmonary thromboembolism (PTE) is a common and often life-threatening complication associated with a variety of ……………….and ……………. diseases. A thrombus formed in the ………… heart or the …………….. or ………… venous system can embolize to the pulmonary arterial vasculature.
Pulmonary thromboembolism (PTE) is a common and often life-threatening complication associated with a variety of systemic and metabolic diseases. A thrombus formed in the right heart or the peripheral or central venous system can embolize to the pulmonary arterial vasculature.
PTE occurs in several disease states associated with hypercoagulability including ………..syndrome, …………., immune-mediated ………….. ……………., ………………….., ……………… disease, sepsis, ……………………………., ………….. disease, and ………………..
nephrotic syndrome,
hyperadrenocorticism,
immune-mediated hemolytic anemia,
thrombocytosis,
cardiac disease,
sepsis,
disseminated intravascular coagulation,
heartworm disease,
neoplasia.
………………… III deficiency may be involved in thrombogenesis as part of a number of these diseases.
For example, destruction of red blood cells in immune-mediated hemolytic anemia releases ………………. substances.
Antithrombin III deficiency may be involved in thrombogenesis as part of a number of these diseases.
For example, destruction of red blood cells in immune-mediated hemolytic anemia releases thrombogenic substances.
Antithrombin III inactivates ………….. and other ………………, and only mild reduction in ………… can result in thrombosis or thromboembolism.
Antithrombin III inactivates thrombin and other clotting factors, and only mild reduction in AT-III can result in thrombosis or thromboembolism.
A deficiency of AT-III can be secondary to decreased ………… (e.g., congenital), increased …………. (e.g., DIC), loss of …………………………. from the intravascular compartment (e.g., nephrotic syndrome), and increased …………… catabolism (e.g., Cushing’s disease).
A deficiency of AT-III can be secondary to decreased synthesis (e.g., congenital), increased consumption (e.g., DIC), loss of antithrombin from the intravascular compartment (e.g., nephrotic syndrome), and increased protein catabolism (e.g., Cushing’s disease).
Protein … and protein …. are vitamin K–dependent protein factors and major inhibitors of the ……………………
……………… of both of these proteins have been associated with clinical thrombotic disorders in humans.
Protein C and protein S are vitamin K–dependent protein factors and major inhibitors of the procoagulant system.
Deficiencies of both of these proteins have been associated with clinical thrombotic disorders in humans.
The presence of multiple concurrent disorders in patients with thromboembolism is common. For example, 47% of cats with necropsy confirmed PTE had multiple concurrent predisposing disorders.[24] PTE is covered in detail in Chapter 233.
The presence of multiple concurrent disorders in patients with thromboembolism is common. For example, 47% of cats with necropsy confirmed PTE had multiple concurrent predisposing disorders.[24] PTE is covered in detail in Chapter 233.
Varicosis and ulceration are rare in dogs and cats. When detected, they often accompany arteriovenous fistulas. Cutaneous phlebectasia is a benign lesion sometimes erroneously called telangiectasis. It is reported almost exclusively in dogs with spontaneous or iatrogenic Cushing’s syndrome. Phlebectasia is an abnormal dilatation, extension, or reduplication of veins or capillaries or a combination of these changes.
Varicosis and ulceration are rare in dogs and cats. When detected, they often accompany arteriovenous fistulas. Cutaneous phlebectasia is a benign lesion sometimes erroneously called telangiectasis. It is reported almost exclusively in dogs with spontaneous or iatrogenic Cushing’s syndrome. Phlebectasia is an abnormal dilatation, extension, or reduplication of veins or capillaries or a combination of these changes.
Venous perforation or blunt trauma to veins is usually well tolerated because rapid clotting results in venous occlusion. If when venous occlusion or venous severance is severe, however, resultant edema and cyanosis are usually temporary because of collateral circulation. If all veins draining an area are compromised, marked edema and necrosis can ensue. Blunt trauma has been associated with caudal vena caval obstruction or kinking of the intrathoracic caudal vena cava and ascites.
Venous perforation or blunt trauma to veins is usually well tolerated because rapid clotting results in venous occlusion. If when venous occlusion or venous severance is severe, however, resultant edema and cyanosis are usually temporary because of collateral circulation. If all veins draining an area are compromised, marked edema and necrosis can ensue. Blunt trauma has been associated with caudal vena caval obstruction or kinking of the intrathoracic caudal vena cava and ascites.
Venous malformations have been previously referred to as cavernous hemangiomas. They can be localized or extensive and appear as cystic dilation of blood vessels. They generally permit only low blood flow and small lesions are generally asymptomatic. Expansion of the lesion may occur, however, especially following trauma. Thrombosis may occur due to sluggish blood flow, resulting in local swelling and tenderness. Larger lesions in dependent areas may enlarge, causing significant vascular dilation. This may result in changes in skin color, ulceration, and hemorrhage. Affected area appears as a warm, soft, compressible mass. No thrills or bruits are present due to the low flow. Pain may result from pressure exerted on deep tissues and nerves. Diagnosis is made using history, physical examination, and ultrasound. Venography may be necessary to define the lesion. Symptomatic therapy using light, compressive wraps is sometimes helpful for acute management. Surgical excision of affected vessels is occasionally required, but complete resection is difficult and local recurrence is common.
Venous malformations have been previously referred to as cavernous hemangiomas. They can be localized or extensive and appear as cystic dilation of blood vessels. They generally permit only low blood flow and small lesions are generally asymptomatic. Expansion of the lesion may occur, however, especially following trauma. Thrombosis may occur due to sluggish blood flow, resulting in local swelling and tenderness. Larger lesions in dependent areas may enlarge, causing significant vascular dilation. This may result in changes in skin color, ulceration, and hemorrhage. Affected area appears as a warm, soft, compressible mass. No thrills or bruits are present due to the low flow. Pain may result from pressure exerted on deep tissues and nerves. Diagnosis is made using history, physical examination, and ultrasound. Venography may be necessary to define the lesion. Symptomatic therapy using light, compressive wraps is sometimes helpful for acute management. Surgical excision of affected vessels is occasionally required, but complete resection is difficult and local recurrence is common.
Venous aneurysms are rare in veterinary medicine with only a few reported cases. Two cases have been identified in the dog: one case report of a dog with an aneurysm of the jugular, linguofacial, and maxillary veins and a second dog with a cranial vena cava aneurysm.[28],[29] In both cases, these lesions were considered to be secondary to a congenital vascular anomaly and not associated with an obstructive or traumatic process. Thrombosis commonly follows blunt trauma and perforating injuries, particularly with venipuncture or prolonged venous catheterization (Figure 256-2)
Venous aneurysms are rare in veterinary medicine with only a few reported cases. Two cases have been identified in the dog: one case report of a dog with an aneurysm of the jugular, linguofacial, and maxillary veins and a second dog with a cranial vena cava aneurysm.[28],[29] In both cases, these lesions were considered to be secondary to a congenital vascular anomaly and not associated with an obstructive or traumatic process. Thrombosis commonly follows blunt trauma and perforating injuries, particularly with venipuncture or prolonged venous catheterization (Figure 256-2)
…………………. is a major cause of intimal damage leading to thrombosis. The thrombosis is usually of little local consequence. However, emboli may be carried to the lung and cause PTE. In most animals, blood clots carried to the lung are rapidly lysed and cause no problems. However, when inflammatory diseases, dehydration, or circulatory failure occurs, clot formation may continue in the pulmonary vessels and lead to vascular occlusion, severe dyspnea, pain, and death.
Phlebitis is a major cause of intimal damage leading to thrombosis. The thrombosis is usually of little local consequence. However, emboli may be carried to the lung and cause PTE. In most animals, blood clots carried to the lung are rapidly lysed and cause no problems. However, when inflammatory diseases, dehydration, or circulatory failure occurs, clot formation may continue in the pulmonary vessels and lead to vascular occlusion, severe dyspnea, pain, and death.
In ……………………… thrombophlebitis, bacterial emboli may be carried to the lungs and cause thromboembolic pneumonia. Spontaneous venous thrombosis is rare, although portal vein thrombosis has been reported. Clinical signs include ascites, peripheral pitting edema, and portosystemic shunting.
In infectious thrombophlebitis, bacterial emboli may be carried to the lungs and cause thromboembolic pneumonia. Spontaneous venous thrombosis is rare, although portal vein thrombosis has been reported. Clinical signs include ascites, peripheral pitting edema, and portosystemic shunting.
Embolization of severed intravascular catheter……………. is an occasional complication of intravenous catheter placement. In humans, reported complications of catheter embolization include perforation of cardiac walls, endocarditis, pulmonary embolism, and severe arrhythmias.
Therefore, it is generally considered prudent to removal catheter fragments. Nonsurgical, transvenous removal of catheter fragments using loop-snare catheters, forceps, and basket catheters have been described. Whenever possible, however, steps should be taken to avoid situations predisposing to catheter fragmentation including inadequate restraint during catheter placement, withdrawal of catheters through their placement needles during repositioning, failure to properly secure catheter to the patient, and inadvertent severing of catheters during bandage changes.
Embolization of severed intravascular catheter fragments is an occasional complication of intravenous catheter placement. In humans, reported complications of catheter embolization include perforation of cardiac walls, endocarditis, pulmonary embolism, and severe arrhythmias.
Therefore, it is generally considered prudent to removal catheter fragments. Nonsurgical, transvenous removal of catheter fragments using loop-snare catheters, forceps, and basket catheters have been described. Whenever possible, however, steps should be taken to avoid situations predisposing to catheter fragmentation including inadequate restraint during catheter placement, withdrawal of catheters through their placement needles during repositioning, failure to properly secure catheter to the patient, and inadvertent severing of catheters during bandage changes.
Phlebitis can occur from a local inflammatory process extending to the veins or can originate from a venous intimal lesion. Common causes of venous intimal lesions are perivenous injection of irritating drugs, infusion of large amounts of fluid, and long-term placement of intravenous catheters. Infusion-related phlebitis occurs in three forms: (1) chemical (injury to vein by irritating drugs), (2) physical (trauma to the intima by catheters, needles, hypertonicity or particulate matter in infused fluids), and (3) microbial (infected fluids, skin, or catheter tip). Sterile or septic thrombophlebitis may result. It usually remains localized and is characterized by pain, swelling, and exudation (Figure 256-3). Patients with serious illnesses or compromised immune systems, however, may develop sepsis, thromboembolic pneumonia, or endocarditis.
Phlebitis can occur from a local inflammatory process extending to the veins or can originate from a venous intimal lesion. Common causes of venous intimal lesions are perivenous injection of irritating drugs, infusion of large amounts of fluid, and long-term placement of intravenous catheters. Infusion-related phlebitis occurs in three forms: (1) chemical (injury to vein by irritating drugs), (2) physical (trauma to the intima by catheters, needles, hypertonicity or particulate matter in infused fluids), and (3) microbial (infected fluids, skin, or catheter tip). Sterile or septic thrombophlebitis may result. It usually remains localized and is characterized by pain, swelling, and exudation (Figure 256-3). Patients with serious illnesses or compromised immune systems, however, may develop sepsis, thromboembolic pneumonia, or endocarditis.